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2-苄基-2,3,4,5-四氢-1H-吡啶并[4,3-b]吲哚

更新时间:2025-09-02 21:15:29

2-苄基-2,3,4,5-四氢-1H-吡啶并[4,3-b]吲哚结构式
2-苄基-2,3,4,5-四氢-1H-吡啶并[4,3-b]吲哚结构式
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常用名 2-苄基-2,3,4,5-四氢-1H-吡啶并[4,3-b]吲哚 英文名 {1H-Pyrido[4,3-b]indole,} 2,3,4,5-tetrahydro-2-(phenylmethyl)
CAS号 6208-43-1 分子量 262.34900
密度 1.203g/cm3 沸点 425ºC at 760 mmHg
分子式 C18H18N2 熔点 N/A
MSDS N/A 闪点 210.8ºC

 2-苄基-2,3,4,5-四氢-1H-吡啶并[4,3-b]吲哚名称

中文名 2-苄基-2,3,4,5-四氢-1H-吡啶并[4,3-b]吲哚
英文名 2-benzyl-1,3,4,5-tetrahydropyrido[4,3-b]indole
英文别名 更多

 2-苄基-2,3,4,5-四氢-1H-吡啶并[4,3-b]吲哚物理化学性质

密度 1.203g/cm3
沸点 425ºC at 760 mmHg
分子式 C18H18N2
分子量 262.34900
闪点 210.8ºC
精确质量 262.14700
PSA 19.03000
LogP 3.66410
InChIKey TWZCZLLZJDKWFN-UHFFFAOYSA-N
SMILES c1ccc(CN2CCc3[nH]c4ccccc4c3C2)cc1
折射率 1.69

 2-苄基-2,3,4,5-四氢-1H-吡啶并[4,3-b]吲哚合成线路

~93%

2-苄基-2,3,4,5-四氢-1H-吡啶并[4,3-b]吲哚结构式

2-苄基-2,3,4,5-四氢...

6208-43-1

文献:AMGEN INC.; BREGMAN, Howard; BUCHANAN, John, L.; CHAKKA, Nagasree; DIMAURO, Erin, F.; DU, Bingfan; NGUYEN, Hanh, Nho; ZHENG, Xiao, Mei Patent: WO2011/103196 A1, 2011 ; Location in patent: Page/Page column 83 ; WO 2011/103196 A1

~%

2-苄基-2,3,4,5-四氢-1H-吡啶并[4,3-b]吲哚结构式

2-苄基-2,3,4,5-四氢...

6208-43-1

文献:USTAV EXPIREMENTALNEJ FARMAKOLOGIE A TOXIKOLOGIE SAV; SNIRC, Vladimir; BUCHMAN, Marek; STEFEK, Milan; BAUER, Viktor; STOLC, Svorad; MIHALOVA, Danica; PATOPRSTY, Vladimir; POVAZANEC, Frantisek Patent: WO2011/139242 A2, 2011 ; Location in patent: Page/Page column 12-13 ;

~95%

2-苄基-2,3,4,5-四氢-1H-吡啶并[4,3-b]吲哚结构式

2-苄基-2,3,4,5-四氢...

6208-43-1

文献:Kudzma, Linas V. Synthesis, 2003 , # 11 p. 1661 - 1666

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2-苄基-2,3,4,5-四氢-1H-吡啶并[4,3-b]吲哚结构式

2-苄基-2,3,4,5-四氢...

6208-43-1

文献:Kudzma, Linas V. Synthesis, 2003 , # 11 p. 1661 - 1666

~%

2-苄基-2,3,4,5-四氢-1H-吡啶并[4,3-b]吲哚结构式

2-苄基-2,3,4,5-四氢...

6208-43-1

文献:Kudzma, Linas V. Synthesis, 2003 , # 11 p. 1661 - 1666

~%

2-苄基-2,3,4,5-四氢-1H-吡啶并[4,3-b]吲哚结构式

2-苄基-2,3,4,5-四氢...

6208-43-1

文献:Smolyar; Volchkov; Yutilov Pharmaceutical Chemistry Journal, 2001 , vol. 35, # 9 p. 514 - 517

~%

2-苄基-2,3,4,5-四氢-1H-吡啶并[4,3-b]吲哚结构式

2-苄基-2,3,4,5-四氢...

6208-43-1

文献:Smolyar; Volchkov; Yutilov Pharmaceutical Chemistry Journal, 2001 , vol. 35, # 9 p. 514 - 517

~%

2-苄基-2,3,4,5-四氢-1H-吡啶并[4,3-b]吲哚结构式

2-苄基-2,3,4,5-四氢...

6208-43-1

文献:Bridoux, Alexandre; Millet, Regis; Pommery, Jean; Pommery, Nicole; Henichart, Jean-Pierre Bioorganic and Medicinal Chemistry, 2010 , vol. 18, # 11 p. 3910 - 3924

 2-苄基-2,3,4,5-四氢-1H-吡啶并[4,3-b]吲哚靶点实验

查看更多实验

实验名称:Luminescence-based cell-based primary high throughput screening assay to identify ago...
来源:The Scripps Research Institute Molecular Screening Center
靶标:mu-type opioid receptor isoform MOR-1 [Homo sapiens]
External Id:OPRM1-OPRD1_AG_LUMI_1536_1X%ACT PRUN
实验名称:QFRET-based biochemical primary high throughput screening assay to identify exosite i...
来源:The Scripps Research Institute Molecular Screening Center
靶标:disintegrin and metalloproteinase domain-containing protein 17 preproprotein [Homo sapiens]
External Id:ADAM17_INH_QFRET_1536_1X%INH PRUN
实验名称:Fluorescence-based cell-based primary high throughput screening assay to identify ago...
来源:The Scripps Research Institute Molecular Screening Center
靶标:muscarinic acetylcholine receptor M1 [Homo sapiens]
External Id:CHRM1_AG_FLUO8_1536_1X%ACT PRUN
实验名称:qHTS for Inhibitors of human tyrosyl-DNA phosphodiesterase 1 (TDP1): qHTS in cells in...
来源:NCGC
靶标:TDP1 protein [Homo sapiens]
External Id:TDP1100
实验名称:qHTS for Inhibitors of human tyrosyl-DNA phosphodiesterase 1 (TDP1): qHTS in cells in...
来源:NCGC
靶标:TDP1 protein [Homo sapiens]
External Id:TDP1101
实验名称:Schnurri-3 Inhibitors: specific inducers of adult bone formation Measured in Cell-Bas...
来源:Broad Institute
靶标:N/A
External Id:2134-01_Inhibitor_SinglePoint_HTS_Activity_Set2
实验名称:Fluorescence polarization to screen for inhibitor that competite the binding of FadD2...
来源:Broad Institute
靶标:FATTY-ACID-CoA LIGASE FADD28 (FATTY-ACID-CoA SYNTHETASE)
External Id:2147-01_Inhibitor_SinglePoint_HTS_Activity
实验名称:Bursicon-induced LGR2 mediated cAMP production in LGR-2/CRE6x-Luciferase co-transfect...
来源:Broad Institute
靶标:N/A
External Id:Bursicon-induced LGR2 mediated cAMP production in LGR-2/CRE6x-Luciferase co-transfected HEK293 cells Inhibition - 7011-01_Antagonist_SinglePoint_HTS_Activity
实验名称:qHTS for Inhibitors of AMA1-RON; Towards Development of Antimalarial Drug Lead: Prima...
来源:NCGC
靶标:apical membrane antigen 1, AMA1 [Plasmodium falciparum 3D7]
External Id:AMA1100
实验名称:Fluorescence polarization-based biochemical high throughput primary assay to identify...
来源:The Scripps Research Institute Molecular Screening Center
靶标:abhydrolase domain-containing protein 4 isoform 1 [Mus musculus]
External Id:ABHD4_INH_FP_1536_1X%INH PRUN
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 2-苄基-2,3,4,5-四氢-1H-吡啶并[4,3-b]吲哚英文别名

2-Benzyl-2,3,4,5-tetrahydro-1H-pyrido(4,3-b)indole
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